T-regulatory cells in severe atopic dermatitis: alterations related to cytokines and other lymphocyte subpopulations
The changes in lymphocyte subpopulations in atopic dermatitis (AD) concern also T-regulatory cells. We investigated the expression of various surface receptors on CD3 + CD4 + CD25 high FoxP3 + T-regulatory cells and the activation CD28 + receptor and the inhibitory CD152 + receptor on helper/inducer...
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Published in | Archives of Dermatological Research Vol. 304; no. 10; pp. 795 - 801 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer-Verlag
01.12.2012
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Abstract | The changes in lymphocyte subpopulations in atopic dermatitis (AD) concern also T-regulatory cells. We investigated the expression of various surface receptors on CD3
+
CD4
+
CD25
high
FoxP3
+
T-regulatory cells and the activation CD28
+
receptor and the inhibitory CD152
+
receptor on helper/inducer as well as cytotoxic/suppressor T cells. Peripheral blood lymphocytes of 15 AD patients and 20 healthy subjects were analyzed by flow cytometry using monoclonal antibodies. The concentrations of IL-6, IL-10 and TGF-β were determined in the serum and the supernatant of ConA-stimulated CD4
+
lymphocytes. In AD patients the percentage of CD4
+
CD25
high
FoxP3
+
as well as CD3
+
CD8
+
cells increased, which positively correlated with SCORAD index (
r
= 0.55,
p
= 0.03). The concentrations of IL-10 in the CD4
+
lymphocyte culture supernatants and the concentrations of TGF-β in the sera and the supernatant negatively correlated with the severity of AD (
p
< 0.01,
r
= −0.63;
p
< 0.02,
r
= −0.64 and
p
< 0.03,
r
= −0.58, respectively), whereas the serum concentration of IL-6 correlated positively (
p
< 0.003,
r
= 0.71). The regulatory cells expressed more CD62L and CD134 surface markers but less CD95. Reduced expression of the apoptotic CD95 receptor suggests that survival time of these cells is prolonged. Since CD62L and CD134 were upregulated, the enhanced modulatory effect of CD4
+
CD25
high
FoxP3
+
cells seemed to be suggested, which may result in increased co-expression of CD28/CD152 on both CD4
+
and CD8
+
subpopulations. |
---|---|
AbstractList | The changes in lymphocyte subpopulations in atopic dermatitis (AD) concern also T-regulatory cells. We investigated the expression of various surface receptors on CD3 super(+)CD4 super(+)CD25 super(high)FoxP3 super(+) T-regulatory cells and the activation CD28 super(+) receptor and the inhibitory CD152 super(+) receptor on helper/inducer as well as cytotoxic/suppressor T cells. Peripheral blood lymphocytes of 15 AD patients and 20 healthy subjects were analyzed by flow cytometry using monoclonal antibodies. The concentrations of IL-6, IL-10 and TGF- beta were determined in the serum and the supernatant of ConA-stimulated CD4 super(+) lymphocytes. In AD patients the percentage of CD4 super(+)CD25 super(high)F oxP3 super(+) as well as CD3 super(+)CD8 super(+) cells increased, which positively correlated with SCORAD index (r = 0.55, p = 0.03). The concentrations of IL-10 in the CD4 super(+) lymphocyte culture supernatants and the concentrations of TGF- beta in the sera and the supernatant negatively correlated with the severity of AD (p < 0.01, r = -0.63; p < 0.02, r = -0.64 and p < 0.03, r = -0.58, respectively), whereas the serum concentration of IL-6 correlated positively (p < 0.003, r = 0.71). The regulatory cells expressed more CD62L and CD134 surface markers but less CD95. Reduced expression of the apoptotic CD95 receptor suggests that survival time of these cells is prolonged. Since CD62L and CD134 were upregulated, the enhanced modulatory effect of CD4 super(+)CD25 super(high)F oxP3 super(+) cells seemed to be suggested, which may result in increased co-expression of CD28/CD152 on both CD4 super(+) and CD8 super(+) subpopulations. The changes in lymphocyte subpopulations in atopic dermatitis (AD) concern also T-regulatory cells. We investigated the expression of various surface receptors on CD3(+)CD4(+)CD25(high)FoxP3(+) T-regulatory cells and the activation CD28(+) receptor and the inhibitory CD152(+) receptor on helper/inducer as well as cytotoxic/suppressor T cells. Peripheral blood lymphocytes of 15 AD patients and 20 healthy subjects were analyzed by flow cytometry using monoclonal antibodies. The concentrations of IL-6, IL-10 and TGF-β were determined in the serum and the supernatant of ConA-stimulated CD4(+) lymphocytes. In AD patients the percentage of CD4(+)CD25(high)FoxP3(+) as well as CD3(+)CD8(+) cells increased, which positively correlated with SCORAD index (r = 0.55, p = 0.03). The concentrations of IL-10 in the CD4(+) lymphocyte culture supernatants and the concentrations of TGF-β in the sera and the supernatant negatively correlated with the severity of AD (p < 0.01, r = -0.63; p < 0.02, r = -0.64 and p < 0.03, r = -0.58, respectively), whereas the serum concentration of IL-6 correlated positively (p < 0.003, r = 0.71). The regulatory cells expressed more CD62L and CD134 surface markers but less CD95. Reduced expression of the apoptotic CD95 receptor suggests that survival time of these cells is prolonged. Since CD62L and CD134 were upregulated, the enhanced modulatory effect of CD4(+)CD25(high)FoxP3(+) cells seemed to be suggested, which may result in increased co-expression of CD28/CD152 on both CD4(+) and CD8(+) subpopulations.The changes in lymphocyte subpopulations in atopic dermatitis (AD) concern also T-regulatory cells. We investigated the expression of various surface receptors on CD3(+)CD4(+)CD25(high)FoxP3(+) T-regulatory cells and the activation CD28(+) receptor and the inhibitory CD152(+) receptor on helper/inducer as well as cytotoxic/suppressor T cells. Peripheral blood lymphocytes of 15 AD patients and 20 healthy subjects were analyzed by flow cytometry using monoclonal antibodies. The concentrations of IL-6, IL-10 and TGF-β were determined in the serum and the supernatant of ConA-stimulated CD4(+) lymphocytes. In AD patients the percentage of CD4(+)CD25(high)FoxP3(+) as well as CD3(+)CD8(+) cells increased, which positively correlated with SCORAD index (r = 0.55, p = 0.03). The concentrations of IL-10 in the CD4(+) lymphocyte culture supernatants and the concentrations of TGF-β in the sera and the supernatant negatively correlated with the severity of AD (p < 0.01, r = -0.63; p < 0.02, r = -0.64 and p < 0.03, r = -0.58, respectively), whereas the serum concentration of IL-6 correlated positively (p < 0.003, r = 0.71). The regulatory cells expressed more CD62L and CD134 surface markers but less CD95. Reduced expression of the apoptotic CD95 receptor suggests that survival time of these cells is prolonged. Since CD62L and CD134 were upregulated, the enhanced modulatory effect of CD4(+)CD25(high)FoxP3(+) cells seemed to be suggested, which may result in increased co-expression of CD28/CD152 on both CD4(+) and CD8(+) subpopulations. The changes in lymphocyte subpopulations in atopic dermatitis (AD) concern also T-regulatory cells. We investigated the expression of various surface receptors on CD3^sup +^CD4^sup +^CD25^sup high^FoxP3^sup +^ T-regulatory cells and the activation CD28^sup +^ receptor and the inhibitory CD152^sup +^ receptor on helper/inducer as well as cytotoxic/suppressor T cells. Peripheral blood lymphocytes of 15 AD patients and 20 healthy subjects were analyzed by flow cytometry using monoclonal antibodies. The concentrations of IL-6, IL-10 and TGF-β were determined in the serum and the supernatant of ConA-stimulated CD4^sup +^ lymphocytes. In AD patients the percentage of CD4^sup +^CD25^sup high^FoxP3^sup +^ as well as CD3^sup +^CD8^sup +^ cells increased, which positively correlated with SCORAD index (r = 0.55, p = 0.03). The concentrations of IL-10 in the CD4^sup +^ lymphocyte culture supernatants and the concentrations of TGF-β in the sera and the supernatant negatively correlated with the severity of AD (p < 0.01, r = -0.63; p < 0.02, r = -0.64 and p < 0.03, r = -0.58, respectively), whereas the serum concentration of IL-6 correlated positively (p < 0.003, r = 0.71). The regulatory cells expressed more CD62L and CD134 surface markers but less CD95. Reduced expression of the apoptotic CD95 receptor suggests that survival time of these cells is prolonged. Since CD62L and CD134 were upregulated, the enhanced modulatory effect of CD4^sup +^CD25^sup high^FoxP3^sup +^ cells seemed to be suggested, which may result in increased co-expression of CD28/CD152 on both CD4^sup +^ and CD8^sup +^ subpopulations.[PUBLICATION ABSTRACT] The changes in lymphocyte subpopulations in atopic dermatitis (AD) concern also T-regulatory cells. We investigated the expression of various surface receptors on CD3 + CD4 + CD25 high FoxP3 + T-regulatory cells and the activation CD28 + receptor and the inhibitory CD152 + receptor on helper/inducer as well as cytotoxic/suppressor T cells. Peripheral blood lymphocytes of 15 AD patients and 20 healthy subjects were analyzed by flow cytometry using monoclonal antibodies. The concentrations of IL-6, IL-10 and TGF-β were determined in the serum and the supernatant of ConA-stimulated CD4 + lymphocytes. In AD patients the percentage of CD4 + CD25 high FoxP3 + as well as CD3 + CD8 + cells increased, which positively correlated with SCORAD index ( r = 0.55, p = 0.03). The concentrations of IL-10 in the CD4 + lymphocyte culture supernatants and the concentrations of TGF-β in the sera and the supernatant negatively correlated with the severity of AD ( p < 0.01, r = −0.63; p < 0.02, r = −0.64 and p < 0.03, r = −0.58, respectively), whereas the serum concentration of IL-6 correlated positively ( p < 0.003, r = 0.71). The regulatory cells expressed more CD62L and CD134 surface markers but less CD95. Reduced expression of the apoptotic CD95 receptor suggests that survival time of these cells is prolonged. Since CD62L and CD134 were upregulated, the enhanced modulatory effect of CD4 + CD25 high FoxP3 + cells seemed to be suggested, which may result in increased co-expression of CD28/CD152 on both CD4 + and CD8 + subpopulations. The changes in lymphocyte subpopulations in atopic dermatitis (AD) concern also T-regulatory cells. We investigated the expression of various surface receptors on CD3(+)CD4(+)CD25(high)FoxP3(+) T-regulatory cells and the activation CD28(+) receptor and the inhibitory CD152(+) receptor on helper/inducer as well as cytotoxic/suppressor T cells. Peripheral blood lymphocytes of 15 AD patients and 20 healthy subjects were analyzed by flow cytometry using monoclonal antibodies. The concentrations of IL-6, IL-10 and TGF-β were determined in the serum and the supernatant of ConA-stimulated CD4(+) lymphocytes. In AD patients the percentage of CD4(+)CD25(high)FoxP3(+) as well as CD3(+)CD8(+) cells increased, which positively correlated with SCORAD index (r = 0.55, p = 0.03). The concentrations of IL-10 in the CD4(+) lymphocyte culture supernatants and the concentrations of TGF-β in the sera and the supernatant negatively correlated with the severity of AD (p < 0.01, r = -0.63; p < 0.02, r = -0.64 and p < 0.03, r = -0.58, respectively), whereas the serum concentration of IL-6 correlated positively (p < 0.003, r = 0.71). The regulatory cells expressed more CD62L and CD134 surface markers but less CD95. Reduced expression of the apoptotic CD95 receptor suggests that survival time of these cells is prolonged. Since CD62L and CD134 were upregulated, the enhanced modulatory effect of CD4(+)CD25(high)FoxP3(+) cells seemed to be suggested, which may result in increased co-expression of CD28/CD152 on both CD4(+) and CD8(+) subpopulations. |
Author | Alifier, Marek Gliński, Wiesław Bodera, Paweł Stankiewicz, Wanda Jurkiewicz, Beata Glińska, Olga Samochocki, Zbigniew Jeziorkowska, Renata Rosiak, Ewa |
Author_xml | – sequence: 1 givenname: Zbigniew surname: Samochocki fullname: Samochocki, Zbigniew email: jdejewska@yahoo.pl organization: Department of Dermatology, Medical University of Warsaw – sequence: 2 givenname: Marek surname: Alifier fullname: Alifier, Marek organization: Department of Clinical Immunology, Medical University in Bialystok – sequence: 3 givenname: Paweł surname: Bodera fullname: Bodera, Paweł organization: Department of Microwave Safety, Military Institute of Hygiene and Epidemiology – sequence: 4 givenname: Renata surname: Jeziorkowska fullname: Jeziorkowska, Renata organization: Department of Dermatology, Medical University of Warsaw – sequence: 5 givenname: Ewa surname: Rosiak fullname: Rosiak, Ewa organization: Department of Microwave Safety, Military Institute of Hygiene and Epidemiology – sequence: 6 givenname: Beata surname: Jurkiewicz fullname: Jurkiewicz, Beata organization: Department of Microwave Safety, Military Institute of Hygiene and Epidemiology – sequence: 7 givenname: Olga surname: Glińska fullname: Glińska, Olga organization: Department of Dermatology, Medical University of Warsaw – sequence: 8 givenname: Wiesław surname: Gliński fullname: Gliński, Wiesław organization: Department of Dermatology, Medical University of Warsaw – sequence: 9 givenname: Wanda surname: Stankiewicz fullname: Stankiewicz, Wanda organization: Department of Microwave Safety, Military Institute of Hygiene and Epidemiology |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22968402$$D View this record in MEDLINE/PubMed |
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Keywords | T-regulatory cells SCORAD index Immunological markers Atopic dermatitis |
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SubjectTerms | Adolescent Adult Antigens, CD - immunology Apoptosis Atopic dermatitis Blood Proteins - metabolism CD134 antigen CD152 antigen CD28 antigen CD4 antigen CD62L protein CD8 antigen CD95 antigen Cell activation Cell culture Cell Separation Cell survival Cytokines Cytokines - immunology Cytotoxicity Dermatitis, Atopic - immunology Dermatitis, Atopic - physiopathology Dermatology Disease Progression Female Flow Cytometry Humans Immunoregulation Interleukin 10 Interleukin 6 Lymphocytes T Male Medicine Medicine & Public Health Monoclonal antibodies Original Paper Peripheral blood Suppressor cells Surface markers T-Lymphocyte Subsets - immunology T-Lymphocytes, Regulatory - immunology Transforming growth factor- beta Young Adult |
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Title | T-regulatory cells in severe atopic dermatitis: alterations related to cytokines and other lymphocyte subpopulations |
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